Clinical Trial Project Manager

Medpace

Cincinnati (OH)

On-site

USD 50,000 - 70,000

Full time

14 days+

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Benefits offered by this job

Flexible work environment

Competitive PTO packages

Competitive compensation and benefits package

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Community involvement with local nonprofit organizations

Discounts on local sports games, fitness gyms and attractions

Modern, ecofriendly campus with an on-site fitness center

Structured career paths

Discounted tuition for UC online programs

Job summary

Medpace in Cincinnati is seeking a Clinical Research professional to manage projects in early phase clinical trials. The role involves overseeing project activities, tracking study progress, and ensuring stakeholder communication. Strong knowledge of medical terminology and clinical research methodology is essential.

The position offers a flexible work environment and is part of a company that values employee wellness and community involvement. Benefits include competitive PTO and support for professional development.

Qualifications

1-3 years of research-related experience.
Broad knowledge of medical terminology and clinical research methodology.

Responsibilities

Manage one or more projects according to Sponsor specifications.
Coordinate project start-up, maintenance, and close-out activities.
Track study status including patient status, case report form status, safety issues, timelines.
Serve as primary contact for all protocol interpretations and logistical project-related issues.
Provide oversight for staff conducting study-related responsibilities/procedures.

Skills

Knowledge of medical terminology

Clinical research methodology

Education

Bachelor’s Degree

Job description

Job Summary

Medpace Clinical Pharmacology, a 96-bed facility specializing in early phase clinical trials, is led by a team of highly trained clinical researchers who are experts in the design, implementation, and analysis of Phase I - IIa studies. The Phase I Unit, functionally integrated with Medpace, a large global Clinical Research Organization, conducts studies and collaborates with the best therapeutic minds in the industry to bring promising drug compounds to the market.

Responsibilities

Responsible for managing one or more projects according to Sponsor specifications;
Coordinate project start-up, maintenance, and close-out activities;
Track study status including patient status, case report form status, safety issues, timelines, etc.;
Serve as primary contact for all protocol interpretations and logistical project-related issues; and
Provide oversight for staff conducting study-related responsibilities/procedures.

Qualifications